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Terminology chevron_right Concepts chevron_right 773666007

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Component

773666007

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)

Shortest Term

Hạ đường huyết giảm insulin máu và phì đại nửa người

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)

SCTID: 773666007, Primitive, Active

773666007|Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)|

vi Hạ đường huyết giảm insulin máu và phì đại nửa người
en Hypoinsulinemic hypoglycaemia and body hemihypertrophy
en Hypoinsulinemic hypoglycemia and body hemihypertrophy
en Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)

Expression

773666007 |Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)|
 <<< 363104002 |Hereditary disorder of endocrine system (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
52767006 |Neonatal hypoglycemia (disorder)| + 
736653007 |Neonatal disorder of endocrine system (disorder)| + 
123762005 |Hypoinsulinism (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 363698007 |Finding site (attribute)| = 78696007 |Endocrine pancreatic structure (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 434912009 |Blood glucose concentration (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
453451000003119 - hạ đường huyết giảm insulin máu và phì đại nửa người (vi) View
453451000003119	vi	Synonym (core metadata concept)	hạ đường huyết giảm insulin máu và phì đại nửa người	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3725582014 - Hypoinsulinemic hypoglycaemia and body hemihypertrophy (en) View
3725582014	en	Synonym (core metadata concept)	Hypoinsulinemic hypoglycaemia and body hemihypertrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3725580018 - Hypoinsulinemic hypoglycemia and body hemihypertrophy (en) View
3725580018	en	Synonym (core metadata concept)	Hypoinsulinemic hypoglycemia and body hemihypertrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3725581019 - Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder) (en) View
3725581019	en	Fully specified name (core metadata concept)	Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10610345029) - 773666007 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12876749021) - 773666007 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12206036023) - 773666007 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12206037025) - 773666007 -> 434912009 (363714003) View
363714003 \|Interprets (attribute)\|	434912009 \|Blood glucose concentration (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610338029) - 773666007 -> 78696007 (363698007) View
363698007 \|Finding site (attribute)\|	78696007 \|Endocrine pancreatic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610339021) - 773666007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610340023) - 773666007 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610341022) - 773666007 -> 52767006 (116680003) View
116680003 \|Is a (attribute)\|	52767006 \|Neonatal hypoglycemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610342026) - 773666007 -> 736653007 (116680003) View
116680003 \|Is a (attribute)\|	736653007 \|Neonatal disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610343020) - 773666007 -> 123762005 (116680003) View
116680003 \|Is a (attribute)\|	123762005 \|Hypoinsulinism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10610344025) - 773666007 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
736653007 View
736653007	Neonatal disorder of endocrine system (disorder)	Neonatal endocrine disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
52767006 View
52767006	Neonatal hypoglycemia (disorder)	Neonatal hypoglycemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
123762005 View
123762005	Hypoinsulinism (disorder)	Hypoinsulinism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (a4ed3cc5-7153-501e-93c3-00e12f03fb32) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.3	TRUE	ALWAYS Q87.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (ecea7663-3c06-5cb8-9864-39627b903626) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E34.8	TRUE	ALWAYS E34.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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